Oral, ultra-long-lasting drug delivery: Application toward malaria elimination goals

被引:194
作者
Bellinger, Andrew M. [1 ,2 ,3 ,4 ]
Jafari, Mousa [1 ,2 ]
Grant, Tyler M. [1 ,2 ,4 ]
Zhang, Shiyi [1 ,2 ,13 ]
Slater, Hannah C. [5 ]
Wenger, Edward A. [6 ]
Mo, Stacy [1 ,2 ]
Lee, Young-Ah Lucy [1 ,2 ]
Mazdiyasni, Hormoz [1 ,2 ]
Kogan, Lawrence [1 ,2 ]
Barman, Ross [1 ,2 ]
Cleveland, Cody [1 ,2 ,7 ]
Booth, Lucas [1 ,2 ]
Bensel, Taylor [1 ,2 ]
Minahan, Daniel [1 ,2 ]
Hurowitz, Haley M. [1 ,2 ]
Tai, Tammy [1 ,2 ]
Daily, Johanna [8 ]
Nikolic, Boris [9 ]
Wood, Lowell
Eckhoff, Philip A. [6 ]
Langer, Robert [1 ,2 ,10 ,11 ]
Traverso, Giovanni [1 ,2 ,7 ,12 ]
机构
[1] MIT, Dept Chem Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Brigham & Womens Hosp, Harvard Med Sch, Dept Med, Div Cardiovasc, 75 Francis St, Boston, MA 02115 USA
[4] Lyndra Inc, Watertown, MA 02472 USA
[5] Imperial Coll London, MRC Ctr Outbreak Anal & Modelling, Dept Infect Dis Epidemiol, London, England
[6] Inst Dis Modeling, Bellevue, WA 98005 USA
[7] Brigham & Womens Hosp, Harvard Med Sch, Div Gastroenterol, 75 Francis St, Boston, MA 02115 USA
[8] Albert Einstein Coll Med, Div Infect Dis, Bronx, NY 10461 USA
[9] Biomat Capital, 1107 1st Ave,Apartment 1305, Seattle, WA 98101 USA
[10] MIT, Media Lab, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[11] MIT, Inst Med Engn & Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[12] Massachusetts Gen Hosp, Harvard Med Sch, Div Gastroenterol, Boston, MA 02114 USA
[13] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai, Peoples R China
关键词
PLASMODIUM-FALCIPARUM MALARIA; GASTRIC RESIDENCE TIMES; LYMPHATIC FILARIASIS; IVERMECTIN; TRANSMISSION; FEASIBILITY; AFRICA; BURDEN; IMPACT; SAFETY;
D O I
10.1126/scitranslmed.aag2374
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Efforts at elimination of scourges, such as malaria, are limited by the logistic challenges of reaching large rural populations and ensuring patient adherence to adequate pharmacologic treatment. We have developed an oral, ultra-long-acting capsule that dissolves in the stomach and deploys a star-shaped dosage form that releases drug while assuming a geometry that prevents passage through the pylorus yet allows passage of food, enabling prolonged gastric residence. This gastric-resident, drug delivery dosage form releases small-molecule drugs for days to weeks and potentially longer. Upon dissolution of the macrostructure, the components can safely pass through the gastrointestinal tract. Clinical, radiographic, and endoscopic evaluation of a swine large-animal model that received these dosage forms showed no evidence of gastrointestinal obstruction or mucosal injury. We generated long-acting formulations for controlled release of ivermectin, a drug that targets malaria-transmitting mosquitoes, in the gastric environment and incorporated these into our dosage form, which then delivered a sustained therapeutic dose of ivermectin for up to 14 days in our swine model. Further, by using mathematical models of malaria transmission that incorporate the lethal effect of ivermectin against malaria-transmitting mosquitoes, we demonstrated that this system will boost the efficacy of mass drug administration toward malaria elimination goals. Encapsulated, gastric-resident dosage forms for ultra-long-acting drug delivery have the potential to revolutionize treatment options for malaria and other diseases that affect large populations around the globe for which treatment adherence is essential for efficacy.
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页数:12
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